DUSP16
dual specificity phosphatase 16
Summary
This gene encodes a mitogen-activated protein kinase phosphatase that is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. The encoded protein specifically regulates the c-Jun amino-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) pathways.[provided by RefSeq, May 2010]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs148434374 | 12:12,629,798 | G/A | — | uncertain significance |
| rs1192495973 | 12:12,629,867 | C/A | — | uncertain significance |
| rs532656810 | 12:12,629,892 | G/A | — | uncertain significance |
| rs753562199 | 12:12,629,973 | G/A | — | uncertain significance |
| rs778782615 | 12:12,629,985 | C/T | — | uncertain significance |
| rs201126170 | 12:12,630,050 | A/G | — | uncertain significance |
| rs762374205 | 12:12,630,065 | T/C | — | uncertain significance |
| rs372167746 | 12:12,630,122 | G/A | — | uncertain significance |
| rs764920091 | 12:12,630,179 | G/A | — | uncertain significance |
| rs797005926 | 12:12,630,213 | G/A | — | uncertain significance |
| rs142808469 | 12:12,630,308 | G/A | — | uncertain significance |
| rs762231755 | 12:12,630,410 | G/C | — | uncertain significance |
| rs1424094765 | 12:12,630,453 | C/T | — | uncertain significance |
| rs112390593 | 12:12,630,607 | G/A | — | likely benign |
| rs200573264 | 12:12,630,641 | G/A | — | uncertain significance |
| rs2111269 | 12:12,630,685 | C/T | — | likely benign |
| rs762082661 | 12:12,630,690 | T/C | — | uncertain significance |
| rs772280915 | 12:12,630,693 | C/T | — | uncertain significance |
| rs1425928935 | 12:12,630,723 | C/T | — | uncertain significance |
| rs1235968998 | 12:12,630,777 | C/T | — | uncertain significance |
| rs773448870 | 12:12,630,785 | G/A | — | uncertain significance |
| rs779911001 | 12:12,630,840 | T/C | — | uncertain significance |
| rs1363964104 | 12:12,630,849 | C/G | — | uncertain significance |
| rs199660192 | 12:12,630,857 | C/T | — | uncertain significance |
| rs772174638 | 12:12,630,875 | T/A | — | uncertain significance |
| rs10845554 | 12:12,632,950 | G/C | intron variant | — |
| rs61758451 | 12:12,633,204 | G/A | — | likely benign |
| rs372821072 | 12:12,639,990 | C/A | — | likely benign |
| rs370518275 | 12:12,640,030 | C/T | — | uncertain significance |
| rs1943696422 | 12:12,640,040 | G/A | — | uncertain significance |
| rs753103309 | 12:12,640,046 | C/T | — | uncertain significance |
| rs150403725 | 12:12,653,490 | T/C | — | uncertain significance |
| rs1943894663 | 12:12,653,563 | T/C | — | uncertain significance |
| rs11612508 | 12:12,657,513 | A/C | — | — |
| rs747726 | 12:12,670,227 | G/A | intron variant | — |
| rs773437147 | 12:12,672,834 | T/C | — | uncertain significance |
| rs187382315 | 12:12,672,941 | T/G | — | benign |
| rs746432264 | 12:12,673,815 | G/A | — | uncertain significance |
| rs929637584 | 12:12,673,962 | T/C | — | uncertain significance |
| rs1244921478 | 12:12,673,992 | C/T | — | uncertain significance |
| rs2498025815 | 12:12,674,006 | T/G | — | uncertain significance |
| rs139487616 | 12:12,674,026 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.